Подписаться
Jackie de Belleroche
Jackie de Belleroche
Professor of Neuroscience, Imperial College London
Подтвержден адрес электронной почты в домене imperial.ac.uk
Название
Процитировано
Процитировано
Год
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1
DJ Klionsky, AK Abdel-Aziz, S Abdelfatah, M Abdellatif, A Abdoli, S Abel, ...
autophagy 17 (1), 1-382, 2021
107042021
TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis
J Sreedharan, IP Blair, VB Tripathi, X Hu, C Vance, B Rogelj, S Ackerley, ...
Science 319 (5870), 1668-1672, 2008
29752008
Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6
C Vance, B Rogelj, T Hortobágyi, KJ De Vos, AL Nishimura, J Sreedharan, ...
Science 323 (5918), 1208-1211, 2009
29652009
Endoplasmic reticulum stress signalling–from basic mechanisms to clinical applications
A Almanza, A Carlesso, C Chintha, S Creedican, D Doultsinos, B Leuzzi, ...
The FEBS journal 286 (2), 241-278, 2019
7102019
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
5762018
A locus on chromosome 9p confers susceptibility to ALS and frontotemporal dementia
M Morita, A Al-Chalabi, PM Andersen, B Hosler, P Sapp, E Englund, ...
Neurology 66 (6), 839-844, 2006
4592006
Exome-wide rare variant analysis identifies TUBA4A mutations associated with familial ALS
BN Smith, N Ticozzi, C Fallini, AS Gkazi, S Topp, KP Kenna, EL Scotter, ...
Neuron 84 (2), 324-331, 2014
4112014
Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase
J Mitchell, P Paul, HJ Chen, A Morris, M Payling, M Falchi, J Habgood, ...
Proceedings of the National Academy of Sciences 107 (16), 7556-7561, 2010
2982010
NEK1 variants confer susceptibility to amyotrophic lateral sclerosis
KP Kenna, PTC Van Doormaal, AM Dekker, N Ticozzi, BJ Kenna, ...
Nature genetics 48 (9), 1037-1042, 2016
2822016
Protection of neuronal cells from apoptosis by Hsp27 delivered with a herpes simplex virus-based vector
MJD Wagstaff, Y Collaço-Moraes, J Smith, JS de Belleroche, RS Coffin, ...
Journal of Biological Chemistry 274 (8), 5061-5069, 1999
2681999
The C9ORF72 expansion mutation is a common cause of ALS+/− FTD in Europe and has a single founder
BN Smith, S Newhouse, A Shatunov, C Vance, S Topp, L Johnson, ...
European Journal of Human Genetics 21 (1), 102-108, 2013
2542013
Metabolism of beds of mammalian cortical synaptosomes: response to depolarizing influences
JS De Belleroche, HF Bradford
Journal of neurochemistry 19 (3), 585-602, 1972
2541972
Differential expression of 14 genes in amyotrophic lateral sclerosis spinal cord detected using gridded cDNA arrays
A Malaspina, N Kaushik, J De Belleroche
Journal of neurochemistry 77 (1), 132-145, 2001
2512001
Cyclooxygenase‐2 induction in cerebral cortex: an intracellular response to synaptic excitation
J Adams, Y Collaço‐Moraes, J De Belleroche
Journal of neurochemistry 66 (1), 6-13, 1996
2421996
Analysis of gene expression in two large schizophrenia cohorts identifies multiple changes associated with nerve terminal function
PR Maycox, F Kelly, A Taylor, S Bates, J Reid, R Logendra, MR Barnes, ...
Molecular psychiatry 14 (12), 1083-1094, 2009
2252009
CCNF mutations in amyotrophic lateral sclerosis and frontotemporal dementia
KL Williams, S Topp, S Yang, B Smith, JA Fifita, ST Warraich, KY Zhang, ...
Nature communications 7 (1), 11253, 2016
2192016
Characterization of the properties of a novel mutation in VAPB in familial amyotrophic lateral sclerosis
HJ Chen, G Anagnostou, A Chai, J Withers, A Morris, J Adhikaree, ...
Journal of Biological Chemistry 285 (51), 40266-40281, 2010
2082010
The neuroprotective effects of heat shock protein 27 overexpression in transgenic animals against kainate-induced seizures and hippocampal cell death
MT Akbar, AMC Lundberg, K Liu, S Vidyadaran, KE Wells, H Dolatshad, ...
Journal of Biological Chemistry 278 (22), 19956-19965, 2003
1972003
Identification of PEX7 as the second gene involved in Refsum disease
DM Van Den Brink, P Brites, J Haasjes, AS Wierzbicki, J Mitchell, ...
The American Journal of Human Genetics 72 (2), 471-477, 2003
1932003
Biochemical evidence for the presence of presynaptic receptors on dopaminergic nerve terminals
J De Belleroche, HF Bradford
Brain research 142 (1), 53-68, 1978
1861978
В данный момент система не может выполнить эту операцию. Повторите попытку позднее.
Статьи 1–20